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GPCR/G protein

GPCRs (G-protein coupled receptors) are a major subcategory of signaling pathways that play a crucial role in transmitting signals from outside the cell to within. These receptors are involved in a wide range of physiological processes including sensory perception, neurotransmission, hormonal regulation, and immune responses.

When a ligand binds to a GPCR, it causes a conformational change in the receptor that activates an associated G-protein. The activated G-protein then triggers a cascade of intracellular signaling events that ultimately lead to a specific cellular response.

GPCRs are a diverse family of proteins that can be classified into different subtypes based on their structure and function. Some examples of GPCR subtypes include rhodopsin-like, secretin-like, and metabotropic glutamate receptors.

Dysregulation of GPCR signaling pathways has been implicated in a variety of diseases, including cancer, cardiovascular disorders, and neurological conditions. Therefore, understanding the mechanisms underlying GPCR/G protein signaling is essential for the development of novel therapeutics targeted at these pathways.

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7α,25-dihydroxy Cholesterol, C4241, C27H46O3, GPR183 agonist
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FTY720 Phosphate, C4236, C19H34NO5P, sphingosine-1-phosphate (S1P) receptors agonist
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SQ 29,548, C4237, C21H29N3O4, TP receptor antagonist
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Arachidonoyl amide, C4150, C20H33NO, CB1 receptor agonist
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AG-041R, C4101, C31H36N4O5, gastrin/cholecystokinin-2 (CCKB) receptor antagonist
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W123, C4064, C17H26N2O3, S1P1 antagonist
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CJ-42794, C4037, C22H17ClFNO4, EP4 antagonist
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(±)-4-hydroxy Propranolol (hydrochloride), C4034, C16H21NO3·HCl, β1- and β2-adrenergic receptors inhibitor
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Lofexidine (hydrochloride), C3990, C11H12Cl2N2O·HCl, α2-adrenergic receptor agonist
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Rilmenidine (hemifumarate), C3965, C10H16N2O·1/2C4H4O4, I1-imidazoline binding site selective ligand and α2-adrenoceptor agonist

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